US3993655A - Stabilizers for synthetic polymers - Google Patents

Stabilizers for synthetic polymers Download PDF

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US3993655A
US3993655A US05/525,810 US52581074A US3993655A US 3993655 A US3993655 A US 3993655A US 52581074 A US52581074 A US 52581074A US 3993655 A US3993655 A US 3993655A
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tert
bis
group
butyl
methyl
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Michael Rasberger
Jean Rody
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Novartis Corp
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Ciba Geigy Corp
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
    • C08K5/3432—Six-membered rings
    • C08K5/3435—Piperidines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/40—Oxygen atoms
    • C07D211/44—Oxygen atoms attached in position 4
    • C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/94—Oxygen atom, e.g. piperidine N-oxide

Definitions

  • the invention relates to new derivatives of hydroxybenzylmalonic acids, to their preparation, and to their use as stabilisers for synthetic polymers, as well as to the material stabilised with the aid of the said derivatives.
  • X can be oxygen or --NH--
  • Y represents hydrogen, the radical --O.sup.., an alkyl group having 1 to 12 carbon atoms, an alkenyl group having 3 or 4 carbon atoms, a propargyl group, a benzyl group, or a group of the formula ##STR1## wherein R 6 represents hydrogen, methyl or phenyl, and R 7 represents hydrogen, or an acyl group having up to 18 carbon atoms,
  • R 1 represents a hydroxybenzyl group of formula (II) ##SPC2##
  • R 3 and R 4 each independently represent an alkyl group having 1 to 8 carbon atoms, and R 5 represents hydrogen or methyl, and
  • R 2 represents, if X is oxygen, hydrogen or a hydroxybenzyl group of formula (II); if, however, X is --NH--, only hydrogen.
  • Y denotes an alkyl group
  • it can be a primary alkyl group, such as, e.g. a methyl, ethyl, n-propyl, n-butyl, n-hexyl, n-octyl, n-decyl or n-dodecyl group.
  • R 3 and R 4 can have the same meaning as R, but in addition represent a secondary or tertiary alkyl group, such as, e.g. a isopropyl, sec.butyl, 2-ethylhexyl, tert.butyl or tert.octyl group.
  • Y represents an alkenyl group
  • it can be, for example, an allyl or methallyl group.
  • R 7 can be an aliphatic acyl group, for example, an acetyl, propionyl hexanoyl, acryl, methacryl, 2-ethyl-hexanoyl, dodecanoyl or octadecanoyl group, and also an aromatic acyl group, especially a benzoyl group.
  • the said new compounds of formula I constitute a molecular combination of these two structures.
  • the new compounds Compared with a mixture of an anti-oxidant of the hydroxybenzylmalonic acid series and a light stabiliser of the tetramethylpiperidine series, the new compounds have the advantage of a more simple incorporation and of an overall uniformly constant ratio of anti-oxidant to light stabiliser.
  • these new compounds have a greater stabilising action than that of the same amount of a mixture of a hydroxybenzylmalonic acid derivative and a tetramethylpiperidine derivative. This means in practice that the same effect can be obtained with a smaller amount of stabiliser.
  • the one class is formed by the para-hydroxybenzyl compounds such as those corresponding to formula (I) wherein R 1 represents a group of formula (IIa) ##SPC3##
  • R 3 denotes an isopropyl, tert.butyl or tert.amyl group
  • R 4 denotes a methyl, ethyl, isopropyl, tert.butyl, tert.amyl or tert.octyl group
  • Y in formula (I) represents hydrogen, the radical --O.sup.. or a methyl, allyl or benzyl group.
  • R 3 represents a tertiary butyl group
  • R 4 represents a methyl or tert.butyl group
  • R 5 represents hydrogen
  • Y hydrogen, the radical --O.sup.. or a methyl group.
  • R 3 denotes a tert.butyl, tert.amyl or tert.octyl group
  • Y represents hydrogen, the radical --O.sup.. or a methyl group.
  • Examples of compounds of the first-mentioned class are: bis(3,5-di-tert.butyl-4-hydroxybenzyl)malonic acid-bis (2,2,6,6-tetramethyl-4-piperidinyl)ester, bis(3,5-di-isopropyl-4-hydroxybenyl)malonic acid-bis (2,2,6,6-tetramethyl-4-piperidinyl)ester, bis(3-tert.butyl-4-hydroxy-5-methylbenzyl)malonic acid-bis (2,2,6,6-tetramethyl-4-piperidinyl-1-oxyl)ester, 3,5-di-tert.butyl-4-hydroxybenzylmalonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl-1-oxyl)ester, 3-tert.butyl-4-hydroxy-5,6-dimethylbenzylmalonic acid-bis (2,2,6,6-tetramethyl-4-piperidinyl)ester 3-tert.
  • Examples of compounds of the second-mentioned class are: 4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonic acid-bis-(2,2,6,6-tetramethyl-4-piperidinyl)ester, bis(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)malonic acid-bis(2,2,6,6-tetramethyl-4-piperidinyl)ester, 4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)malonic acid-bis-(2,2,6,6-pentamethyl-4-piperidinyl)ester, bis(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)malonic acid-bis(1,2,2,6,6-pentamethyl-4-piperidinyl)ester, 4-tert.butyl-3-hydroxy-2,6-dimethylbenzylmalonic acid-bis-(2,2,6,6-tetramethyl-4-piperidinyl)
  • the compounds of formula (I) can be prepared by various processes. The most important process comprises the reaction of a malonic acid derivative of formula (III) ##SPC5##
  • Y represents hydrogen, the radical --O.sup.., an alkyl group having 1 to 12 carbon atoms, an alkenyl group having 3 or 4 carbon atoms, a propargyl group, a benzyl group, or a group of the formula ##STR4## wherein R 6 represents hydrogen, methyl or phenyl, and R 7 represents hydrogen, or an acyl group having up to 18 carbon atoms,
  • R 1 represents a hydroxybenzyl group of formula (II) ##SPC6##
  • R 3 and R 4 each independently represent an alkyl group having 1 to 8 carbon atoms
  • R 5 represents hydrogen or methyl
  • R 8 represents an alkyl group having 1 to 5 carbon atoms, or the two radicals R 8 together with the N-atom represent a morpholine, piperidine or pyrrolidine ring.
  • the starting substances of formula (III) are malonic acid esters and malonic acid amides of 4-hydroxy- and 4-aminotetramethylpiperidines, respectively. They are obtainable by standard processes; for example, by base-catalysed transesterification of diethylmalonate with 2 moles of a 4-hydroxy- or 4-aminotetramethylpiperidine.
  • the compounds of formula (IV) are obtainable by reaction of a phenol of the formula R 1 -H with formaldehyde, carbon disulphide and a secondary amine (R 8 ) 2 NH.
  • Suitable basic catalysts are, for example, alkali hydroxides such as NaOH or KOH, alkali or alkaline-earth alcoholates such as CH 3 ONa, C 2 H 5 ONa, (CH 3 ) 3 COK, (C 2 H 5 O) 2 Mg or (CH 3 ) 2 CHOLi, alkali hydrides or alkaline-earth hydrides such as LiH, NaH or CaH 2 , and alkali amides such as NaNH 2 , LiNH 2 or KNH 2 .
  • alkali hydroxides are alkali hydroxides.
  • These bases are preferably employed in equimolar amounts, i.e., per mole of dithiocarbaminate is used one mole-equivalent of the base.
  • Suitable solvents are, for example, alcohols, such as methanol, ethanol, isopropanol or tert.butanol; also suitable are aliphatic ethers or cyclic ethers, such as diethyl ether, tetrahydrofuran or dioxane; also hydrocarbons such as hexane, heptane, ligroin, decalin, cyclohexane, benzene, toluene or xylene, as well as polar aprotic solvents, such as dimethylformamide, dimethylacetamide or dimethylsulphoxide.
  • a further process for the preparation of compounds of formula (I) consists in the reaction of a malonic acid dialkyl ester of formula (VI) with two moles of a tetramethylpiperidine derivative of formula (VII): ##SPC7##
  • R 9 in the formula represents an alkyl radical having 1 to 4 carbon atoms.
  • Suitable bases as catalysts are the same as those described previously. In this process too, the reaction can be performed in a solvent, whereby, with the exception of the alcohols, all the previously mentioned groups of solvents are suitable.
  • reaction is normally performed at elevated temperature, in order to ensure a rapid and complete course of reaction.
  • Isolation of the products can be carried out by the usual methods, for example, by concentration through evaporation, and crystallisation of the residue. It is advantageous for the base to be neutralised before the solvent is distilled off.
  • the compounds of formula (I) can be used as stabilisers for organic polymers.
  • organic polymers are, for example:
  • polyolefins such as polyethylene, which can be optionally cross-linked, polypropylene, polybutene-1, polyisobutene, polymethyl-butene-1, polymethylpentene-1, polyisoprene, polybutadiene, polystyrene, copolymers of the monomers on which the mentioned homopolymers are based, such as ethylene-propylene copolymers, propylene-butene-1 copolymers, propylene-isobutene copolymers, styrene-butadiene copolymers, as well as terpolymers of ethylene and propylene with a diene, such as, e.g.
  • hexadiene, dicyclopentadiene or ethylidenenorbornene mixtures of the above given homopolymers, such as, for example, mixtures of polypropylene and polyethylene, polypropylene and polybutene-1, polypropylene and polyisobutylene, or of butadiene-acrylonitrile copolymerisate with a styrene-butadiene copolymerisate.
  • Halogen-containing vinylpolymers such as polyvinyl chloride, polyvinylidene chloride, polyvinylfluoride, polychloroprene and chlorinated rubbers.
  • Polymers derived from ⁇ , ⁇ -unsaturated acids and their derivatives such as polyacrylates and polymethacrylates, polyacrylamides and polyacrylnitile, as well as copolymers with other vinyl compounds, such as acrylonitrile/butadiene/styrene, acrylonitrile/styrene and acrylonitrile/styrene/acrylic ester copolymers.
  • Polymers derived from unsaturated alcohols and amines or their acyl derivatives or acetals such as polyvinyl alcohol, polyvinyl acetate, polyvinyl stearate, polyvinyl benzoate, polyvinyl maleate, polyvinyl butyral, polyallyl phthalate, polyallyl melamine and their copolymers with other vinyl compounds, such as ethylene/vinyl acetate copolymers.
  • Homopolymers and copolymers derived from epoxides such as polyethylene oxide, or the polymerisates which are derived from bis-glycidyl ethers.
  • Polyacetals such as polyoxymethylene and polyoxyethylene, as well as those polyoxymethylenes which contain ethylene oxide as the comonomer.
  • Polyesters derived from dicarboxylic acids and dialcohols and/or from hydroxycarboxylic acids or the corresponding lactones such as polyethylene glycol terephthalate, polybutylene terephthalate, poly-1,4-dimethylol-cyclohexane terephthalate, as well as their starting materials, such as lower terephthalic acid alkyl esters.
  • Cross-linked polymerisates which are derived from aldehydes on the one hand, and from phenols, ureas and melamines on the other, such as phenol-formaldehyde resins, urea-formaldehyde resins and melamine-formaldehyde resins.
  • Alkyd resins such as glycerin-phthalic acid resins and mixtures thereof with melamine-formaldehyde resins.
  • Unsaturated polyester resins derived from copolyesters of saturated and unsaturated dicarboxylic acids with polyvalent alcohols, as well as vinyl compounds as cross-linking agents, and also their halogen-containing, difficulty combustible modifications.
  • Natural polymers such as cellulose, rubber and proteins, as well as their polymer-homologously chemically modified derivatives, such as cellulose acetates, cellulose propionates and cellulose butyrates, or cellulose ethers, such as methylcellulose.
  • Preferred polymers are polyethylene of high and low density, polypropylene, polybutadiene, polyurethanes, polystyrene and its copolymers, as well as mixtures thereof.
  • the new compounds are added to the substrates in a concentration of 0.01 to 5 percent by weight, calculated on the material to be stabilised.
  • 0.05 to 1.5, particularly preferably 0.1 to 0.8, percent by weight of the compounds, calculated on the material to be stabilised, is incorporated into the said material.
  • Incorporation can be effected after polymerisation; for example, by the mixing of the compounds and, optionally, further additives into the melt, by methods common in practice, before or during moulding (shaping); or by application of the dissolved or dispersed compounds to the polymers, optionally with subsequent removal of the solvent by evaporation.
  • the new compounds can also be added in the form of a master batch, containing these compounds in a concentration of, for example, 2.5 to 25 percent by weight, to the polymers to be stabilised.
  • cross-linking polyethylene the compounds are added before cross-linking.
  • stabilisers may be added to the polymers, or other additives commonly used in plastics technology, such as, e.g. flame-retarding agents, antistatic agents, plasticisers, lubricants, expanding agents, pigments or fillers.
  • test strips The testing of the effectiveness of the additives incorporated in the test strips is performed by heat ageing in an air-circulation furnace at 135° and 149°, with an additive-free test strip serving as a comparison. Three test strips are used from each formulation. The final point is defined as being that at which there commences an easily visible crumbling of the test strip.
  • test strips The testing of the effectiveness of the additives incorporated in the test strips is performed by heat ageing in an air-circulation furnace at 135° and 149°, whereby a test strip containing just the 0.3 part of dilaurylthiodipropionate is taken as a comparison. Three test strips are used from each formulation. The final point is defined as being that at which there commences an easily visible decomposition of the test strip.
  • Example 13 The specimens described in Example 13 were tested also with respect to their colour stability as follows:
  • the resulting mixture is extruded in a laboratory single screw extruder ("Plamvo") at 260° nozzle temperature, 100 r.p.m. and a throughput of 50 g/min, and subsequently granulated.
  • the resulting granulate is spun in a spinning apparatus, with a nozzle temperatue of 280°, into polyfilaments, which are then stretched in the ratio of 1 : 5.5.
  • These filaments are subjected to a gas-fading test analogously to the AATCC Standard 23-1957, the test consisting in the exposure of the specimens to the exhaust gases of a butane-gas burner at 60° for 24 hours.
  • Example 13 From the 1 mm thick test sheets described in Example 13 are cut, with the aid of a Mikrotom, chips (clippings) having a thickness of 25 ⁇ . These clippings are clamped between pieces of stainless-steel mesh, and the thus formed carriers then suspended in an air-circulation furnace and aged at 135° and 147°, respectively. The end point is defined as being the time after which, with slight tapping of the mesh containers, decomposed polypropylene falls out in powder form (control 1-2x daily). The results are given in hours (Table 6).
  • Chips (clippings) 25 ⁇ thick are cut, with the aid of a Mikrotom, from the 1 mm thick test sheets described in Example 14. These clippings are clamped between pieces of stainless-steel mesh, and the thus formed carriers then suspended in an air-circulation furnace and aged at 135° and 147°, respectively. The end point is defined as being the time at which, on slight tapping of the mesh containers, decomposed polypropylene falls out in powder form (control 1-2x daily). The results are given in hours (Table 7).
  • a portion of the moulded sheet thus obtained is cut out and then pressed out between two high-gloss hard aluminium sheets under a hand-hydraulic laboratory press for 6 minutes at 260° with a pressure of 12 tons to give a sheet 0.5 mm in thickness, which is immediately quenched in cold water. From this 0.5 mm sheet is then prepared, under exactly the same conditions, the 0.1 mm thick test sheet material. Specimens each 60 ⁇ 44 mm in size are stamped out from this material and irradiated in the Xenotest 150. These specimens are removed at regular intervals of time from the exposure apparatus and their carbonyl content measured in an IR-spectrophotometer.
  • the increase of the carbonyl extinction on exposure to light is a measure for the photoxidative decomposition of the polymer [cp. L. Balaban et al., J. Polymer Sci. Part C. 22, 1059-1071 (1969); J.F. Heacock, J. Polymer Sci. Part A-1, 22, 2921-34 (1969); D.J. Carlsson and DM. Wiles, Macromolecules 2, 587-606 (1969)] and, as known from experience, is associated with a decline of the mechanical properties of the polymer.
  • the comparison sheet stabilized only with antioxidant
  • ⁇ T denotes the transmission loss with the wave lengths 420 and 680 nm during exposure of the specimens
  • T (560) is the transmission value as a percentage of the value in the case of the unexposed speciment at 560 nm.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US05/525,810 1973-12-10 1974-11-21 Stabilizers for synthetic polymers Expired - Lifetime US3993655A (en)

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JP (1) JPS5817500B2 (enrdf_load_stackoverflow)
AR (1) AR204430A1 (enrdf_load_stackoverflow)
AT (1) AT331522B (enrdf_load_stackoverflow)
AU (1) AU7619474A (enrdf_load_stackoverflow)
BE (1) BE823114A (enrdf_load_stackoverflow)
BR (1) BR7410269A (enrdf_load_stackoverflow)
CA (1) CA1032946A (enrdf_load_stackoverflow)
CH (1) CH589056A5 (enrdf_load_stackoverflow)
DE (1) DE2456864A1 (enrdf_load_stackoverflow)
ES (1) ES432713A1 (enrdf_load_stackoverflow)
FR (1) FR2253742B1 (enrdf_load_stackoverflow)
GB (1) GB1442100A (enrdf_load_stackoverflow)
IL (1) IL46203A0 (enrdf_load_stackoverflow)
IT (1) IT1026868B (enrdf_load_stackoverflow)
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US4110305A (en) * 1971-11-30 1978-08-29 Ciba-Geigy Corporation Polymers stabilized by esters of piperidinols
US4116927A (en) * 1976-07-12 1978-09-26 Argus Chemical Corporation 2,2,6,6-Tetramethyl-4-piperidyl carboxylic acid esters of butane or butene tri carboxylic acids as stabilizers for synthetic polymers
US4131599A (en) * 1975-05-28 1978-12-26 Sankyo Company, Limited Stabilization of poly(mono-olefins)
US4148783A (en) * 1975-12-08 1979-04-10 Ciba-Geigy Corporation Hydroxybenzylmalonic acid derivatives
US4148784A (en) * 1975-12-29 1979-04-10 Ciba-Geigy Corporation Phenol stabilizers
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US4185003A (en) * 1978-02-16 1980-01-22 E. I. Du Pont De Nemours And Company Stabilized copolyetheresters
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US4265803A (en) * 1977-08-08 1981-05-05 Sankyo Company Limited Polymers containing polyalkylpiperidines and use thereof as stabilizers
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US4874391A (en) * 1986-07-29 1989-10-17 Ciba-Geigy Corporation Process for photochemical stabilization of polyamide fiber material and mixtures thereof with other fibers: water-soluble copper complex dye and light-stabilizer
US4892784A (en) * 1988-07-27 1990-01-09 Kimberly-Clark Corporation Surface treatment for inhibiting thermal oxidation of polypropylene fabrics
US5015683A (en) * 1989-03-21 1991-05-14 Ciba-Geigy Corporation Bis(1-hydrocarbyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-amine derivatives and stabilized compositions
US5030243A (en) * 1989-01-05 1991-07-09 Ciba-Geigy Corporation Process for the photochemical stabilization of undyed and dyeable artificial leather with a sterically hindered amine
US5221287A (en) * 1989-06-27 1993-06-22 Ciba-Geigy Corporation Process for the photochemical and thermal stabilization of polyamide fibres having an affinity for acid and basic dyes, and of blends of said fibres with on another and with other fibres
EP0778298A2 (de) 1995-12-07 1997-06-11 Bayer Ag Festkörperreiche Bindemittelkombination
US5932640A (en) * 1989-01-21 1999-08-03 Clariant Finance (Bvi) Limited Dyeability or mass coloration of synthetic polyamide
US6184332B1 (en) 1996-02-29 2001-02-06 Synthopol Chemie Dr. Rer. Pol. Koch Gmbh & Co. Kg Polyester polyols and their use as the polyol component in two-component polyurethane paints
US6187387B1 (en) * 1998-03-19 2001-02-13 Ciba Specialty Chemicals Corporation Stabilization of wood substrates
EP1101780A2 (de) 1999-11-17 2001-05-23 Bayer Ag Neue, festkörperrreiche Bindemittelkombinationen und deren Verwendung
US20050137322A1 (en) * 2003-12-17 2005-06-23 Roesler Richard R. Silane modified two-component polyurethane coating
US20060233973A1 (en) * 2005-04-18 2006-10-19 Konica Minolta Opto, Inc. Cellulose ester film, manufacturing method thereof, optical film, polarizing plate and liquid crystal display
US20090068473A1 (en) * 2005-11-10 2009-03-12 Rudolf Wilhelmus Bernardus Van Wessel Epoxy Based Coatings
US20090270535A1 (en) * 2008-04-24 2009-10-29 3V Sigma S.P.A. Mixtures of sterically hindered amines for the stabilisation of polymers

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DE10322620A1 (de) * 2003-05-20 2004-12-16 Bayer Materialscience Ag Festkörperreiche Bindemittelkombinationen für kratzfeste Decklacke
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US4164480A (en) * 1978-01-09 1979-08-14 Eastman Kodak Company Polychromophoric ultraviolet stabilizers and their use in organic compositions
US4185003A (en) * 1978-02-16 1980-01-22 E. I. Du Pont De Nemours And Company Stabilized copolyetheresters
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US4301061A (en) * 1978-05-18 1981-11-17 Ciba-Geigy Corporation Dibenzodioxaphosphepines and stabilized polymers
US4279720A (en) * 1978-07-13 1981-07-21 Ciba-Geigy Corporation Photocurable composition
US4322527A (en) * 1979-05-15 1982-03-30 Ciba-Geigy Corporation 6-Amino-dibenz[d,g][1,3,2]dioxaphosphocines
US4386204A (en) * 1979-05-15 1983-05-31 Ciba-Geigy Corporation 6-Piperidino-dibenz[d,g][1,3,6,2]dioxathiophosphocine
US4409346A (en) * 1979-05-15 1983-10-11 Ciba-Geigy Corporation Compositions stabilized by 6-amino-dibenz[d,g][1,3,2]dioxaphosphocines
US4377651A (en) * 1979-10-05 1983-03-22 Phillips Petroleum Company Polyolefin stabilization
US4361695A (en) * 1979-11-06 1982-11-30 Montedison S.P.A. Polyesters of N,N-di-alkanol-amines with di-(hydroxy-alkyl-benzyl) malonic acids and use thereof as stabilizers for polymers
US4402983A (en) * 1980-09-19 1983-09-06 E. I. Du Pont De Nemours & Co. Powder coating composition for automotive topcoat
US4496649A (en) * 1982-12-16 1985-01-29 Ciba-Geigy Ag Color-photographic recording material
US4874391A (en) * 1986-07-29 1989-10-17 Ciba-Geigy Corporation Process for photochemical stabilization of polyamide fiber material and mixtures thereof with other fibers: water-soluble copper complex dye and light-stabilizer
US4892784A (en) * 1988-07-27 1990-01-09 Kimberly-Clark Corporation Surface treatment for inhibiting thermal oxidation of polypropylene fabrics
US5030243A (en) * 1989-01-05 1991-07-09 Ciba-Geigy Corporation Process for the photochemical stabilization of undyed and dyeable artificial leather with a sterically hindered amine
US6441088B1 (en) 1989-01-21 2002-08-27 Clariant Finance (Bvi) Limited Polyamide hindered amines
US5932640A (en) * 1989-01-21 1999-08-03 Clariant Finance (Bvi) Limited Dyeability or mass coloration of synthetic polyamide
US5015683A (en) * 1989-03-21 1991-05-14 Ciba-Geigy Corporation Bis(1-hydrocarbyloxy-2,2,6,6-tetramethylpiperidin-4-yl)-amine derivatives and stabilized compositions
US5221287A (en) * 1989-06-27 1993-06-22 Ciba-Geigy Corporation Process for the photochemical and thermal stabilization of polyamide fibres having an affinity for acid and basic dyes, and of blends of said fibres with on another and with other fibres
EP0778298A2 (de) 1995-12-07 1997-06-11 Bayer Ag Festkörperreiche Bindemittelkombination
US6184332B1 (en) 1996-02-29 2001-02-06 Synthopol Chemie Dr. Rer. Pol. Koch Gmbh & Co. Kg Polyester polyols and their use as the polyol component in two-component polyurethane paints
US6187387B1 (en) * 1998-03-19 2001-02-13 Ciba Specialty Chemicals Corporation Stabilization of wood substrates
EP1101780A2 (de) 1999-11-17 2001-05-23 Bayer Ag Neue, festkörperrreiche Bindemittelkombinationen und deren Verwendung
US20050137322A1 (en) * 2003-12-17 2005-06-23 Roesler Richard R. Silane modified two-component polyurethane coating
US20060233973A1 (en) * 2005-04-18 2006-10-19 Konica Minolta Opto, Inc. Cellulose ester film, manufacturing method thereof, optical film, polarizing plate and liquid crystal display
US20090068473A1 (en) * 2005-11-10 2009-03-12 Rudolf Wilhelmus Bernardus Van Wessel Epoxy Based Coatings
US20090270535A1 (en) * 2008-04-24 2009-10-29 3V Sigma S.P.A. Mixtures of sterically hindered amines for the stabilisation of polymers
US7713444B2 (en) 2008-04-24 2010-05-11 3V Sigma S.P.A. Mixtures of sterically hindered amines for the stabilisation of polymers

Also Published As

Publication number Publication date
ATA982174A (de) 1975-11-15
AT331522B (de) 1976-08-25
CH589056A5 (enrdf_load_stackoverflow) 1977-06-30
DE2456864A1 (de) 1975-06-12
BR7410269A (pt) 1976-06-29
ZA747815B (en) 1975-12-31
AU7619474A (en) 1976-06-10
GB1442100A (en) 1976-07-07
DE2456864C2 (enrdf_load_stackoverflow) 1989-03-09
JPS5817500B2 (ja) 1983-04-07
JPS50116529A (enrdf_load_stackoverflow) 1975-09-11
ES432713A1 (es) 1976-12-16
US4221701A (en) 1980-09-09
IT1026868B (it) 1978-10-20
CA1032946A (en) 1978-06-13
SU708995A3 (ru) 1980-01-05
FR2253742B1 (enrdf_load_stackoverflow) 1976-10-22
FR2253742A1 (enrdf_load_stackoverflow) 1975-07-04
AR204430A1 (es) 1976-02-06
SE7413720L (enrdf_load_stackoverflow) 1975-06-11
BE823114A (fr) 1975-06-09
IL46203A0 (en) 1975-03-13
NL7416065A (nl) 1975-06-12

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